Skip to main content
Applied and Environmental Microbiology logoLink to Applied and Environmental Microbiology
. 1996 Nov;62(11):4180–4185. doi: 10.1128/aem.62.11.4180-4185.1996

Autoradiographic Method for Isolation of Diverse Microbial Species with Unique Catabolic Traits

J Dunbar, D Wong, M J Yarus, L J Forney
PMCID: PMC1388982  PMID: 16535444

Abstract

A novel autoradiographic method for isolation of bacteria with unique catabolic traits was developed to overcome many of the limitations of traditional selective enrichment techniques. The method consists of five steps. (i) An environmental sample is directly plated (without enrichment) on a microporous filter atop a solid medium that allows cultivation of diverse kinds of microorganisms. (ii) Once colonies form, two replicas of the filter are prepared and the colonies are regrown. (iii) The replica filters are starved 24 to 72 h to deplete intracellular carbon reserves and then (iv) placed on Na(inf2)(sup35)SO(inf4)-containing solid media with and without a test compound. (v) Following an incubation period, the replica filters are exposed to film in order to identify colonies that incorporate more (sup35)S into cell biomass in the presence of the test compound than in its absence, providing presumptive evidence for metabolism of the compound. The colonies identified in this manner can be recovered from the master filter. To demonstrate this technique, bacteria capable of degrading benzoate were isolated from a single soil slurry by traditional enrichment as well as by autoradiography. From the enrichment culture, a single isolate able to degrade benzoate was obtained. In contrast, 18 distinct strains were obtained by purifying 19 putative benzoate-degrading colonies identified by autoradiography. Each of the 18 strains was able to completely transform the substrate, as determined by high-performance liquid chromatography analyses. The doubling times of a subset of the isolates grown in benzoate medium ranged from 1.4 to 17.1 h, whereas the doubling time of the isolate obtained by enrichment was 2.0 h. These data demonstrate that the method described here can be used to obtain a collection of diverse organisms able to metabolize a specific compound.

Full Text

The Full Text of this article is available as a PDF (312.6 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Athiel P., Alfizar, Mercadier C., Vega D., Bastide J., Davet P., Brunel B., Cleyet-Marel J. C. Degradation of iprodione by a soil Arthrobacter-like strain. Appl Environ Microbiol. 1995 Sep;61(9):3216–3220. doi: 10.1128/aem.61.9.3216-3220.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bruce K. D., Hiorns W. D., Hobman J. L., Osborn A. M., Strike P., Ritchie D. A. Amplification of DNA from native populations of soil bacteria by using the polymerase chain reaction. Appl Environ Microbiol. 1992 Oct;58(10):3413–3416. doi: 10.1128/aem.58.10.3413-3416.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. COCHRAN W. G. Estimation of bacterial densities by means of the "most probable number". Biometrics. 1950 Jun;6(2):105–116. [PubMed] [Google Scholar]
  4. Cuhel R. L., Taylor C. D., Jannasch H. W. Assimilatory sulfur metabolism in marine microorganisms: considerations for the application of sulfate incorporation into protein as a measurement of natural population protein synthesis. Appl Environ Microbiol. 1982 Jan;43(1):160–168. doi: 10.1128/aem.43.1.160-168.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Dennis P. P., Bremer H. Macromolecular composition during steady-state growth of Escherichia coli B-r. J Bacteriol. 1974 Jul;119(1):270–281. doi: 10.1128/jb.119.1.270-281.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hanahan D., Meselson M. Plasmid screening at high colony density. Gene. 1980 Jun;10(1):63–67. doi: 10.1016/0378-1119(80)90144-4. [DOI] [PubMed] [Google Scholar]
  7. Harder W., Dijkhuizen L. Strategies of mixed substrate utilization in microorganisms. Philos Trans R Soc Lond B Biol Sci. 1982 Jun 11;297(1088):459–480. doi: 10.1098/rstb.1982.0055. [DOI] [PubMed] [Google Scholar]
  8. Hartmans S., De Bont J. A. Aerobic vinyl chloride metabolism in Mycobacterium aurum L1. Appl Environ Microbiol. 1992 Apr;58(4):1220–1226. doi: 10.1128/aem.58.4.1220-1226.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Heitkamp M. A., Camel V., Reuter T. J., Adams W. J. Biodegradation of p-nitrophenol in an aqueous waste stream by immobilized bacteria. Appl Environ Microbiol. 1990 Oct;56(10):2967–2973. doi: 10.1128/aem.56.10.2967-2973.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Hendricks C. W., Doyle J. D., Hugley B. A new solid medium for enumerating cellulose-utilizing bacteria in soil. Appl Environ Microbiol. 1995 May;61(5):2016–2019. doi: 10.1128/aem.61.5.2016-2019.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Jordan M. J. On counseling minority students in a university center. J Am Coll Health Assoc. 1974 Dec;23(2):146–150. [PubMed] [Google Scholar]
  12. Laguerre G., Allard M. R., Revoy F., Amarger N. Rapid Identification of Rhizobia by Restriction Fragment Length Polymorphism Analysis of PCR-Amplified 16S rRNA Genes. Appl Environ Microbiol. 1994 Jan;60(1):56–63. doi: 10.1128/aem.60.1.56-63.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Li D. Y., Eberspächer J., Wagner B., Kuntzer J., Lingens F. Degradation of 2,4,6-trichlorophenol by Azotobacter sp. strain GP1. Appl Environ Microbiol. 1991 Jul;57(7):1920–1928. doi: 10.1128/aem.57.7.1920-1928.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Loos M. A. Indicator media for microorganisms degrading chlorinated pesticides. Can J Microbiol. 1975 Jan;21(1):104–107. doi: 10.1139/m75-016. [DOI] [PubMed] [Google Scholar]
  15. Matheson V. G., Forney L. J., Suwa Y., Nakatsu C. H., Sexstone A. J., Holben W. E. Evidence for Acquisition in Nature of a Chromosomal 2,4-Dichlorophenoxyacetic Acid/(alpha)-Ketoglutarate Dioxygenase Gene by Different Burkholderia spp. Appl Environ Microbiol. 1996 Jul;62(7):2457–2463. doi: 10.1128/aem.62.7.2457-2463.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Suwa Y., Wright A. D., Fukimori F., Nummy K. A., Hausinger R. P., Holben W. E., Forney L. J. Characterization of a chromosomally encoded 2,4-dichlorophenoxyacetic acid/alpha-ketoglutarate dioxygenase from Burkholderia sp. strain RASC. Appl Environ Microbiol. 1996 Jul;62(7):2464–2469. doi: 10.1128/aem.62.7.2464-2469.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Topp E., Hanson R. S., Ringelberg D. B., White D. C., Wheatcroft R. Isolation and characterization of an N-methylcarbamate insecticide-degrading methylotrophic bacterium. Appl Environ Microbiol. 1993 Oct;59(10):3339–3349. doi: 10.1128/aem.59.10.3339-3349.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Versalovic J., Koeuth T., Lupski J. R. Distribution of repetitive DNA sequences in eubacteria and application to fingerprinting of bacterial genomes. Nucleic Acids Res. 1991 Dec 25;19(24):6823–6831. doi: 10.1093/nar/19.24.6823. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. de Bruijn F. J. Use of repetitive (repetitive extragenic palindromic and enterobacterial repetitive intergeneric consensus) sequences and the polymerase chain reaction to fingerprint the genomes of Rhizobium meliloti isolates and other soil bacteria. Appl Environ Microbiol. 1992 Jul;58(7):2180–2187. doi: 10.1128/aem.58.7.2180-2187.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Applied and Environmental Microbiology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES